Anyone have a neuroendocrine tumor (NET) in the spine?
Does anyone else have a NET in their spine, I cant seem to find anyone? Its just to share experiences and maybe help each other
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
I appreciate hearing "the rest of the story." I've had three carcinoid lesions in the duodenal bulb with surgeries, but no further treatment was needed.
It's so good that you recognize yourself as the "head" of your medical team. I could only wish that all patients were able to take that approach to their treatment and be encouraged to be proactive. It is a good thing to learn as much as possible and ask good questions and help make the best decisions possible for yourself.
As you are comfortable doing so, please keep posting, it is encouraging to others to hear everyone's story.
A question for the group. Like I’ve said I am having a gallium dotatate scan. If the two lesions on my spine are found to be neuroendocrine, I may then proceed to radiation. Does anyone know what the radiation schedule is? How often and for approximately how long? Daily? Weekly? Bi weekly? Etc. Thanks!
You ask a good question, @rrlbees, but unfortunately it is one that no one can answer with any certainty. Each type of lesion is different and therefore are treated differently. Some members who have had radiation for spinal lesions may be able to share their experiences, but it might not reflect what your medical team may suggest that is best for you.
If you feel a need for a second opinion on treatment, you might want to consider a phone/virtual appointment to go over treatment options with a NET specialist.
If you don't mind sharing more, do you have a date scheduled for the scan?
Yes, unfortunately our facility couldn’t get me in until July 19th. I then get my lenreotide injection the next day and visit my oncologist that day also to review the results. I do also have a NET specialist whom I absolutely love. She is Dr Raj at Memorial Sloan Kettering. I will be having the scan slides sent to her for her thoughts also. Then she, my local oncologist and myself will decide on the next steps including consulting with other disciplines such as surgical oncology or radiation oncology etc.
It sounds like you have a great team on your side, @rrlbees. That is so important! I look forward to your updates as you continue this NETs journey.
Thanks. It’s a bit rude of myself to continue to talk about myself and ask questions. But how are you doing?
Thanks for asking, @rrlbees. As far as the NETs issue, everything seems to be stable for now. Some digestive tract side-effects from the surgeries, but that is to be expected. I think of myself as a 20-year survivor as my first surgery was in 2003. A nice anniversary to have!
Quite often for spinal tumors a form of radiation called cyber knife is used. I’m having cyberknife to L4 in a few weeks. Usually there’s 3-5 treatments on consecutive days lasting roughly 1 hour. You will need to have a CT scan so they can map out the treatment. Cyberknife sounds scary but it is like any other radiation however they can deliver higher doses because it is precisely targeted. I’ve had C2, L2,L3 and T12 cyberknifed and since they are all stable. Each cancer responds to radiation differently but it sure beats surgery.
Good Luck
Thank you very much for the info. I have looked a bit at cyber knife and it appears very promising. I realize everyone’s situation is a bit different but this gives me a bit of a heads up in what to expect and discuss if it comes to cyber knife being recommended by my docs.
My husband has a spot on his spine. We are on second round of chemo. 28 day cycle. We are also including red light accupunture and hyperbaric as part of our fight.